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DOI 10.3760/cma.j.cn112139-20230905-00092

Медицинская библиотека · Zhonghua wai ke za zhi [Chinese journal of surgery] · 2024

[Endovascular treatment for Stanford type B aortic dissection in Marfan syndrome patients: a series of 23 cases].

Jiang X L, Liu H, Zou L W, Chen B, Jiang J H, Guo D Q, Xu X, Dong Z H, Fu W G

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Аннотация

Objective

To evaluate the clinical outcomes of thoracic endovascular aortic repair (TEVAR) in the treatment of Stanford type B aortic dissection (TBAD) in Marfan syndrome patients who had no history of aortic arch replacement.

Methods

This is a retrospective case-series study. From January 2009 to December 2019,the clinical data of Marfan syndrome patients who underwent TEVAR for TBAD at the Department of Vascular Surgery were collected. A total of 23 patients were enrolled,including 15 males and 8 females. The age was (38.0±11.0) years (range:24 to 56 years). Among them,12 patients had history of ascending aortic surgery. Details of TEVAR,perioperative complications and reintervention were recorded and survival rate was analyzed by Kaplan-Meier curve.

Results

Technical success was 91.3% (21/23). Two patients with technical failure were as follows:one patient had type Ⅰa endoleak at the completion angiography,which healed spontaneously during the follow-up,and the other patient suffered aortic intimal intussusception after the deployment of the first stent-graft, and the second stent-graft was deployed. However, type Ⅲ endoleak was detected,which disappeared during the follow-up. One patient died during hospitalization. The median follow-up time (M(IQR)) was 60 (48) months (range:12 to 132 months). Reintervention was performed on 7 patients,including 3 distal stent-graft-induced new entry,2 distal aortic dilation,1 Ⅰa endoleak and 1 retrograde type A aortic dissection,respectively. Five-year cumulative survival rate was 86.7% (95%CI:86.6% to 86.8%) and the 5-year freedom from reintervention rate was 81.8% (95%CI:61.8% to 92.8%).

Conclusions

TEVAR is feasible in the treatment of TBAD in Marfan syndrome patients who has no history of aortic arch replacement. It has high technical success rate and low perioperative complication.

Для цитирования: Jiang X L, Liu H, Zou L W, Chen B, Jiang J H, Guo D Q, Xu X, Dong Z H, Fu W G. [Endovascular treatment for Stanford type B aortic dissection in Marfan syndrome patients: a series of 23 cases].. Zhonghua wai ke za zhi [Chinese journal of surgery]. 2024. DOI: 10.3760/cma.j.cn112139-20230905-00092.

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